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Feasibility clinical trial of the combination of AloCelyvir with chemotherapy and radiotherapy for the treatment of children and adolescents with relapsed or refractory extracranial solid tumors.

Status
Not yet recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-518417-25-00
Acronym
FIBHNJ-2019-01
Enrollment
24
Registered
2024-10-10
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Relapsed or refractory extracranial solid tumors in children and adolescents.

Brief summary

Dose confirmation phase: Rate of dose-limiting toxicities.

Detailed description

Expansion phase: Rate of objective responses (complete and partial responses) of the combination., Feasibility of the combination: rate of patients who meet selection criteria who can receive at least one cycle of the combination of Alo-Celyvir with chemo-radiotherapy and measurement of the time from recruitment to the preparation and administration of Alo-Celyvir., Dose confirmation phase: Rate of objective responses (complete and partial responses) of the combination., Progression free survival., Global survival., Rate of adverse events.

Interventions

Sponsors

Fundacion Para La Investigacion Biomedica Hospital Infantil Universitario Nino Jesus
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
0 Years to 64 Years

Design outcomes

Primary

MeasureTime frame
Dose confirmation phase: Rate of dose-limiting toxicities.

Secondary

MeasureTime frame
Expansion phase: Rate of objective responses (complete and partial responses) of the combination., Feasibility of the combination: rate of patients who meet selection criteria who can receive at least one cycle of the combination of Alo-Celyvir with chemo-radiotherapy and measurement of the time from recruitment to the preparation and administration of Alo-Celyvir., Dose confirmation phase: Rate of objective responses (complete and partial responses) of the combination., Progression free survival., Global survival., Rate of adverse events.

Countries

Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026